Product NDC: | 51670-100 |
Proprietary Name: | RECURO VAGINAL |
Non Proprietary Name: | POVIDONE IODINE |
Active Ingredient(s): | .3 mL/100mL & nbsp; POVIDONE IODINE |
Administration Route(s): | VAGINAL |
Dosage Form(s): | DOUCHE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51670-100 |
Labeler Name: | IONA PHARMACY |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101025 |
Package NDC: | 51670-100-01 |
Package Description: | 1 BOTTLE in 1 BOX (51670-100-01) > 10 mL in 1 BOTTLE |
NDC Code | 51670-100-01 |
Proprietary Name | RECURO VAGINAL |
Package Description | 1 BOTTLE in 1 BOX (51670-100-01) > 10 mL in 1 BOTTLE |
Product NDC | 51670-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | POVIDONE IODINE |
Dosage Form Name | DOUCHE |
Route Name | VAGINAL |
Start Marketing Date | 20101025 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | IONA PHARMACY |
Substance Name | POVIDONE-IODINE |
Strength Number | .3 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |